Evidence map›Paper›PMID 42570979›Full record

ArticleHepatology international2026

HBV RNA, HBcrAg, and HBsAg levels at year 6 do not predict HCC risk in patients with cirrhosis on long-term entecavir therapy.

Hung-Hsuan Pan, Tung-Hung Su, Tsung-Hui Hu, Wan-Long Chuang, Wei-Wen Su, Chun-Che Lin, Cheng-Yuan Peng, Chia-Chi Wang, Yao-Chun Hsu, Yi-Wen Huang and 11 more

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Article in Hepatology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

21 authors.

Hung-Hsuan PanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Tung-Hung SuDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan. tunghungsu@ntu.edu.tw.
Tsung-Hui HuDivision of Hepatogastroenterology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Wan-Long ChuangDepartment of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Wei-Wen SuDivision of Gastroenterology and Hepatology, Department of Internal Medicine Changhua Christian Hospital, Changhua, Taiwan.
Chun-Che LinDivision of Gastroenterology, Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan.
Cheng-Yuan PengCenter for Digestive Medicine, Department of Internal Medicine, China Medical University Hospital, China Medical University, Taichung, Taiwan.
Chia-Chi WangDivision of Gastroenterology, Department of Internal Medicine, Taipei Tzuchi Hospital, The Buddhist Tzuchi Medical Foundation, Taipei, Taiwan.
Yao-Chun HsuDepartment of Medical Research, E-Da Hospital, Kaohsiung, Taiwan.
Yi-Wen HuangLiver Center, Cathay General Hospital Medical Center, Taipei, Taiwan.
Kuo-Chih TsengDepartment of Internal Medicine, Dalin Tzu Chi Hospital, Chiayi, Taiwan.
Chih-Lin LinDepartment of Gastroenterology, Ren-Ai Branch, Taipei City Hospital, Taipei, Taiwan.
Sheng-Shun YangDivision of Gastroenterology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Fat-Moon SukDivision of Gastroenterology, Department of Internal Medicine, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan.
Shih-Jer HsuDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Tsung-Ming ChenDivision of Hepato-Gastroenterology, Department of Internal Medicine, and Department of Medical Research, Tungs' Taichung MetroHarbor Hospital, Taichung, Taiwan.
Ming-Jong BairDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Mackay Memorial Hospital, Taitung, Taiwan.
Cheng-Kuan LinDepartment of Internal Medicine, Far Eastern Memorial Hospital, Taipei, Taiwan.
Tai-Chung TsengDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Jia-Horng KaoDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan. kaojh@ntu.edu.tw.ORCID http://orcid.org/0000-0002-2442-7952
C-TEAM study group and the Taiwan Liver Diseases Consortium

Funding

Ministry of Health and Welfare MOHW114-TDU-B-221-144003National Science and Technology Council NSTC 113-2314-B-002-243National Science and Technology Council NSTC 114-2314-B-002 -243 -MY3National Taiwan University 113M7054National Taiwan University Hospital 114-CTC0032National Taiwan University Hospital 114-TMU17National Taiwan University Hospital VN114-08
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe prognostic value of on-treatment hepatitis B virus (HBV) RNA, hepatitis B core-related antigen (HBcrAg), and quantitative hepatitis B surface antigen (HBsAg) for hepatocellular carcinoma (HCC) risk in patients with chronic hepatitis B (CHB) remains uncertain. We evaluate the predictive roles of these viral markers in patients with CHB receiving long-term entecavir therapy.

methodsThis prospective, multicenter study enrolled patients with CHB-related cirrhosis undergoing long-term entecavir treatment and HCC surveillance in Taiwan. Serum HBV RNA, HBcrAg, and HBsAg levels were measured at enrollment. Multivariable regression identified predictors of HBV RNA positivity and HCC development.

resultsOverall, 451 patients were included. After a median of 6.2 years of antiviral therapy, the median levels of HBV RNA, HBcrAg, and HBsAg were 0.9 log10 copies/mL, 3.2 log10 U/mL, and 2.4 log10 IU/mL, respectively. During a median 3.3-year follow-up, 55 developed HCC. 57.2% of patients had detectable HBV RNA. HBV RNA detectability was associated with older age, lower alanine aminotransferase (ALT), HBeAg positivity, and higher HBsAg and HBcrAg levels. In multivariable analysis, higher fibrosis-4 (FIB-4) index (adjusted subdistribution hazard ratio [aSHR], 1.10; 95% confidence interval [CI] 1.00-1.21) and elevated alpha-fetoprotein (AFP) (aSHR, 1.01; 95% CI 1.00-1.01) independently predicted HCC development, whereas the three viral markers did not.

conclusionAfter a 6-year entecavir therapy, 57.2% of patients with CHB-related cirrhosis had detectable HBV RNA. Year-6 HBV RNA, HBcrAg, and HBsAg levels were not predictive of HCC, while FIB-4 index and AFP remained independent predictors.

Indexed as

CirrhosisHBcrAgHBsAgHBV RNAHepatitis BLiver cancer

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.